Canonical Allele Identifier: CA1528949068

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871422T= , CM000667.2:g.14871422T=	GRCh38
NC_000005.9:g.14871531T= , CM000667.1:g.14871531T=	GRCh37
NC_000005.8:g.14924531T=	NCBI36
NG_008273.1:g.5357A=
NG_008273.2:g.5364A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.26A= MANE Select	ENSP00000284268.6:p.His9=
ENST00000284268.6:c.26A=	ENSP00000284268.6:p.His9=
ENST00000505140.1:c.26A=	ENSP00000426332.1:p.His9=
ENST00000513115.1:n.51A=
NM_054027.4:c.26A=	NP_473368.1:p.His9=
XM_011514067.1:c.26A=	XP_011512369.1:p.His9=
NM_054027.5:c.26A=	NP_473368.1:p.His9=
NM_054027.6:c.26A= MANE Select	NP_473368.1:p.His9=